Highly active and durable chemically ordered Pt-Fe-Co intermetallics as cathode catalysts of membrane-electrode assemblies in polymer electrolyte fuel cells
A cathode catalyst with enhanced activity for the oxygen reduction reaction and high durability is greatly required in polymer electrolyte fuel cells (PEFCs). We report that chemically ordered intermetallics, Pt sub(2)FeCo/C with L1 sub(0) ordered structure and Pt sub(6)FeCo/C with L1 sub(2) ordered...
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Veröffentlicht in: | Journal of power sources 2014-12, Vol.271, p.346-353 |
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Sprache: | eng |
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Zusammenfassung: | A cathode catalyst with enhanced activity for the oxygen reduction reaction and high durability is greatly required in polymer electrolyte fuel cells (PEFCs). We report that chemically ordered intermetallics, Pt sub(2)FeCo/C with L1 sub(0) ordered structure and Pt sub(6)FeCo/C with L1 sub(2) ordered structure, achieve both higher activity in solution and higher durability as the cathode catalyst of a membrane-electrode assembly (MEA) under actual PEFC operating conditions, compared with a commercial Pt/C. The mass activity of Pt sub(2)FeCo/C is about twice as high as that of a commercial Pt/C, and Pt sub(6)FeCo/C has a slightly higher mass activity than a commercial Pt/C in solution. These intermetallics were evaluated for durability as the cathodes of MEAs. During the load cycle durability test, the electrochemical surface area (ECSA) of Pt sub(2)FeCo/C is retained, while that of Pt sub(6)FeCo/C decreases, although less than a commercial Pt/C. The retention of ECSA is consistent with smaller changes in the particle size, observed with transmission electron microscopy, of the intermetallics than of a commercial Pt/C. X-ray diffraction patterns after the durability test show that while some part of ordered intermetallics is transformed into pure Pt, the chemically ordered structure of Pt sub(2)FeCo/C is largely retained. Highly active and durable ordered intermetallics are oromisinz as cathode catalvsts of PEFCs. |
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ISSN: | 0378-7753 1873-2755 |
DOI: | 10.1016/j.jpowsour.2014.08.005 |